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Coping Strategies for Chronic Pain
N/A
Recruiting
Led By Dokyoung S You, PhD
Research Sponsored by Stanford University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Prescription opioid use (>3 months)
Chronic pain ( > 3months)
Must not have
Other severe psychiatric conditions (schizophrenia, delusional disorder, psychotic disorder, dissociative disorder, and active suicidality)
Any skin conditions on the hand (pain testing site)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at day 14 (7 days after intervention)
Awards & highlights
No Placebo-Only Group
Summary
This trial will test whether pain catastrophizing is a possible treatment target to reduce prescription opioid craving.
Who is the study for?
This trial is for adults over 18 with chronic pain lasting more than 3 months who have been using prescription opioids. Participants must speak English and have access to email or a smartphone. People with cancer, severe psychiatric conditions, concurrent psychological therapy, skin conditions on the hand, or without technology access cannot join.
What is being tested?
The study tests if 'pain catastrophizing'—a negative mental approach to pain—can be reduced to lessen opioid craving in chronic pain patients. It will also explore if stress hormones and negative emotions are part of why this might work.
What are the potential side effects?
Since this intervention involves coping statements rather than medication, traditional side effects like those seen with drugs are not expected. However, participants may experience emotional discomfort when addressing their thoughts about pain.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have been using prescribed opioids for more than 3 months.
Select...
I have been experiencing pain for more than 3 months.
Select...
I am 18 years old or older.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I do not have severe psychiatric conditions like schizophrenia or active thoughts of suicide.
Select...
I have a skin condition on my hand.
Select...
I am currently diagnosed with cancer.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ at day 14 (7 days after intervention)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at day 14 (7 days after intervention)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
craving
Secondary study objectives
Anxiety symptoms
Cortisol
Depression symptoms
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Coping statementExperimental Treatment1 Intervention
Daily practice of pain coping statements for 7 days
Group II: ControlActive Control1 Intervention
No instruction about pain coping statement.
Find a Location
Who is running the clinical trial?
Stanford UniversityLead Sponsor
2,491 Previous Clinical Trials
17,518,989 Total Patients Enrolled
39 Trials studying Chronic Pain
9,853 Patients Enrolled for Chronic Pain
National Institute on Drug Abuse (NIDA)NIH
2,605 Previous Clinical Trials
3,329,762 Total Patients Enrolled
64 Trials studying Chronic Pain
84,114 Patients Enrolled for Chronic Pain
Dokyoung S You, PhDPrincipal InvestigatorStanford University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have been using prescribed opioids for more than 3 months.I have been experiencing pain for more than 3 months.I do not have severe psychiatric conditions like schizophrenia or active thoughts of suicide.I am 18 years old or older.I have a skin condition on my hand.I am currently receiving psychological therapy.I am currently diagnosed with cancer.
Research Study Groups:
This trial has the following groups:- Group 1: Coping statement
- Group 2: Control
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.